Literature DB >> 26096079

Gaining momentum: New options and opportunities for the treatment of advanced melanoma.

Olivier Michielin1, Christoph Hoeller2.   

Abstract

Before 2011, patients with advanced or metastatic melanoma had a particularly poor long-term prognosis. Since traditional treatments failed to confer a survival benefit, patients were preferentially entered into clinical trials of investigational agents. A greater understanding of the epidemiology and biology of disease has underpinned the development of newer therapies, including six agents that have been approved in the EU, US and/or Japan: a cytotoxic T-lymphocyte antigen-4 inhibitor (ipilimumab), two programmed cell death-1 receptor inhibitors (nivolumab and pembrolizumab), two BRAF inhibitors (vemurafenib and dabrafenib) and a MEK inhibitor (trametinib). The availability of these treatments has greatly improved the outlook for patients with advanced melanoma; however, a major consideration for physicians is now to determine how best to integrate these agents into clinical practice. Therapeutic decisions are complicated by the need to consider patient and disease characteristics, and individual treatment goals, alongside the different efficacy and safety profiles of agents with varying mechanisms of action. Long-term survival, an outcome largely out of reach with traditional systemic therapies, is now a realistic goal, creating the additional need to re-establish how clinical benefit is evaluated. In this review we summarise the current treatment landscape in advanced melanoma and discuss the promise of agents still in development. We also speculate on the future of melanoma treatment and discuss how combination and sequencing approaches may be used to optimise patient care in the future.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chemotherapy; Combination; Europe; Immunotherapy; Ipilimumab; Melanoma; Targeted therapy

Mesh:

Substances:

Year:  2015        PMID: 26096079     DOI: 10.1016/j.ctrv.2015.05.012

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  24 in total

1.  An Anti-Programmed Death-1 Antibody (αPD-1) Fusion Protein That Self-Assembles into a Multivalent and Functional αPD-1 Nanoparticle.

Authors:  Peng Zhao; Djordje Atanackovic; Shuyun Dong; Hideo Yagita; Xiao He; Mingnan Chen
Journal:  Mol Pharm       Date:  2017-04-19       Impact factor: 4.939

Review 2.  Optimizing tumor immune response through combination of radiation and immunotherapy.

Authors:  Alissar El Chediak; Ali Shamseddine; Larry Bodgi; Jean-Pierre Obeid; Fady Geara; Youssef H Zeidan
Journal:  Med Oncol       Date:  2017-08-21       Impact factor: 3.064

Review 3.  Advances in immunotherapy for melanoma management.

Authors:  Mohammed Dany; Rose Nganga; Alissar Chidiac; Edith Hanna; Sara Matar; Dirk Elston
Journal:  Hum Vaccin Immunother       Date:  2016-07-25       Impact factor: 3.452

4.  A Novel Plant Sesquiterpene Lactone Derivative, DETD-35, Suppresses BRAFV600E Mutant Melanoma Growth and Overcomes Acquired Vemurafenib Resistance in Mice.

Authors:  Jia-Hua Feng; Kyoko Nakagawa-Goto; Kuo-Hsiung Lee; Lie-Fen Shyur
Journal:  Mol Cancer Ther       Date:  2016-04-05       Impact factor: 6.261

5.  Two Late Recurrences of Conjunctival Melanoma.

Authors:  Niels J Brouwer; Stijn W Genders; Marina Marinkovic; Sjoerd G van Duinen; Martine J Jager; Gré P M Luyten
Journal:  Ocul Oncol Pathol       Date:  2018-12-12

6.  Conjunctival Metastasis of a Cutaneous Melanoma.

Authors:  Niels J Brouwer; Marina Marinkovic; Anouk Jochems; Ellen W Kapiteijn; Sjoerd G van Duinen; Barbara I Haeseker; Martine J Jager; Gregorius P M Luyten
Journal:  Ocul Oncol Pathol       Date:  2017-09-01

Review 7.  Combination or single-agent ipilimumab as immunotherapy of advanced melanoma: a critical review.

Authors:  Omar Abdel-Rahman
Journal:  Melanoma Manag       Date:  2016-08-22

8.  Doublet BRAF/MEK inhibition versus single-agent BRAF inhibition in the management of BRAF-mutant advanced melanoma, biological rationale and meta-analysis of published data.

Authors:  O Abdel-Rahman; H ElHalawani; H Ahmed
Journal:  Clin Transl Oncol       Date:  2015-10-30       Impact factor: 3.405

9.  Climacostol reduces tumour progression in a mouse model of melanoma via the p53-dependent intrinsic apoptotic programme.

Authors:  Cristiana Perrotta; Federico Buonanno; Silvia Zecchini; Alessio Giavazzi; Francesca Proietti Serafini; Elisabetta Catalani; Laura Guerra; Maria Cristina Belardinelli; Simona Picchietti; Anna Maria Fausto; Simone Giorgi; Enrico Marcantoni; Emilio Clementi; Claudio Ortenzi; Davide Cervia
Journal:  Sci Rep       Date:  2016-06-07       Impact factor: 4.379

10.  Unbiased High-Throughput Drug Combination Pilot Screening Identifies Synergistic Drug Combinations Effective against Patient-Derived and Drug-Resistant Melanoma Cell Lines.

Authors:  David A Close; John M Kirkwood; Ronald J Fecek; Walter J Storkus; Paul A Johnston
Journal:  SLAS Discov       Date:  2020-11-18       Impact factor: 3.341

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